| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44819419-44819727 | Common:4; Rare:104; Clinvar (benign):1 | ||||
| chr19:44845943-44846440 | Common:4; Rare:118 | ||||
| chr19:44914489-44914588 | Rare:23 | ||||
| chr19:44954876-44955028 | Common:3; Rare:45 | ||||
| chr19:44955237-44955462 | Common:2; Rare:74 | ||||
| chr19:45038960-45039105 | Rare:51 | ||||
| chr19:45076468-45076593 | Rare:39 | ||||
| chr19:45079130-45079437 | Common:1; Rare:79 | ||||
| chr19:45079630-45079897 | Common:2; Rare:72 | ||||
| chr19:45091502-45091835 | Common:2; Rare:91 | ||||
| chr19:45092817-45093228 | Common:3; Rare:120 | ||||
| chr19:45178626-45178823 | Common:4; Rare:46; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:45251120-45251318 | Common:2; Rare:74 | ||||
| chr19:45370519-45370782 | Common:2; Rare:86; Clinvar:1 | ||||
| chr19:45406079-45406148 | Common:1; Rare:21 |